@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_head
{
this:
np:hasAssertion
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion
;
np:hasProvenance
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance
;
np:hasPublicationInfo
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion
a
np:Assertion
.
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance
a
np:Provenance
.
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion
{
miriam-gene:5519
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN88aee692db259e2735d862b6295f34b2
sio:SIO_000628
miriam-gene:5519
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance
{
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion
dcterms:description
"[These findings indicate that mutations of the PPP2R1B gene are infrequent in ovarian cancer and that deletions affecting the distal portion of chromosome 11q in ovarian cancer likely target inactivation of other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:10935485
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}